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AFM study of the differential inhibitory effects of the green tea polyphenol (-)-epigallocatechin-3-gallate (EGCG) against Gram-positive and Gram-negative bacteria

Authors
Cui, Y.Oh, Y. J.Lim, J.Youn, M.Lee, I.Pak, H. K.Park, W.Jo, W.Park, S.
Issue Date
Feb-2012
Publisher
ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
Keywords
EGCG; H2O2; Atomic force microscopy; Escherichia coli; Staphylococcus aeruginosa
Citation
FOOD MICROBIOLOGY, v.29, no.1, pp.80 - 87
Indexed
SCIE
SCOPUS
Journal Title
FOOD MICROBIOLOGY
Volume
29
Number
1
Start Page
80
End Page
87
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/109039
DOI
10.1016/j.fm.2011.08.019
ISSN
0740-0020
Abstract
(-)-Epigallocatechin-3-gallate (EGCG), a main constituent of tea catechins, affects Gram-positive and Gram-negative bacteria differently; however, the underlying mechanisms are not clearly understood. Atomic force microscopy (AFM) was used to compare morphological alterations in Gram-positive and Gram-negative bacteria induced by EGCG and by H2O2 at sub-minimum inhibitory concentrations (MICs). EGCG initially induced aggregates in the cell envelopes of Staphylococcus aureus and eventually caused cell lysis, which was not observed in cells treated with H2O2. It initially induced nanoscale perforations or microscale grooves in the cell envelopes of Escherichia coli O157:H7 which eventually disappeared, similar to E. coli cells treated with H2O2. An E. coli O157:H7 tpx mutant, with a defect in thioredoxin-dependent thiol peroxidase (Tpx), was more severely damaged by EGCG when compared with its wild type. Similar differing effects were observed in other Gram-positive and Gram-negative bacteria when exposed to EGCG; it caused aggregated in Streptococcus mutans, while it caused grooves in Pseudomonas aeruginosa. AFM results suggest that the major morphological changes of Gram-negative bacterial cell walls induced by EGCG depend on H2O2 release. This is not the case for Gram-positive bacteria. Oxidative stress in Gram-negative bacteria induced by EGCG was confirmed by flow cytometry. (C) 2011 Elsevier Ltd. All rights reserved.
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